Abstract:We report on a novel lithography technique for patterning of hydrogen-passivated amorphous silicon surfaces. A reflection mode scanning near-field optical microscope with uncoated fiber probes has been used to locally oxidize a thin amorphous silicon layer. Lines of 110 nm in width, induced by the optical near field, were observed after etching in potassium hydroxide. The uncoated fibers can also induce oxidation without light exposure, in a manner similar to an atomic force microscope, and linewidths of 50 nm… Show more
“…Since the sample is illuminated through an uncoated fiber probe, we have previously proposed that the narrow central peak is due to the optical near-field emitted from the very end of the SNOM probe, whereas the broader side peaks are due to an optical interference pattern mainly dominated by the far-field penetrating the sidewalls of the uncoated probe. 10 The full width at halfmaximum of the central peak is ϳ115 nm. The typical linewidth of the side peaks is 215-225 nm, and the average peak-to-peak distance between the central peak and the side peaks is 245 nm.…”
Section: A Lithography With Uncoated Fiber Probesmentioning
confidence: 99%
“…De-convoluting the shape of the AFM tip, the actual linewidth may be as narrow as 35 m. Also, we do not observe any oxidation when the light to the probe is switched off, in contrast to unexpected oxidation effects that have been reported previously with uncoated fiber probes under no illumination. 10 …”
Section: B Lithography With Aluminum-coated Fiber Probesmentioning
confidence: 99%
“…4,8 More recently, optically induced hydrogen desorption was reported. [9][10][11] In this article we discuss results obtained using a scanning near-field optical microscope ͑SNOM͒ 12 to generate an oxide mask on an amorphous silicon ͑a-Si͒ layer. Results for uncoated fiber probes are compared with those for aluminum-coated probes.…”
Section: Introductionmentioning
confidence: 99%
“…Line scans with an uncoated fiber display a three-peak profile after etching the surface in potassium hydroxide ͑KOH͒. 10 Numerical simulations based on a macroscopic self-consistent model 13,14 have been used to explain the experimental observations. Taking the uncertainty of the precise shape of the probe into account, the model was found to be in good agreement with the observed silicon structures.…”
Optically induced oxidation of hydrogen-passivated silicon surfaces using a scanning near-field optical microscope was achieved with both uncoated and aluminum-coated fiber probes. Line scans on amorphous silicon using uncoated fiber probes display a three-peak profile after etching in potassium hydroxide. Numerical simulations of the electromagnetic field around the probe–sample interaction region are used to explain the experimental observations. With an aluminum-coated fiber probe, lines of 35 nm in width were transferred into the amorphous silicon layer.
“…Since the sample is illuminated through an uncoated fiber probe, we have previously proposed that the narrow central peak is due to the optical near-field emitted from the very end of the SNOM probe, whereas the broader side peaks are due to an optical interference pattern mainly dominated by the far-field penetrating the sidewalls of the uncoated probe. 10 The full width at halfmaximum of the central peak is ϳ115 nm. The typical linewidth of the side peaks is 215-225 nm, and the average peak-to-peak distance between the central peak and the side peaks is 245 nm.…”
Section: A Lithography With Uncoated Fiber Probesmentioning
confidence: 99%
“…De-convoluting the shape of the AFM tip, the actual linewidth may be as narrow as 35 m. Also, we do not observe any oxidation when the light to the probe is switched off, in contrast to unexpected oxidation effects that have been reported previously with uncoated fiber probes under no illumination. 10 …”
Section: B Lithography With Aluminum-coated Fiber Probesmentioning
confidence: 99%
“…4,8 More recently, optically induced hydrogen desorption was reported. [9][10][11] In this article we discuss results obtained using a scanning near-field optical microscope ͑SNOM͒ 12 to generate an oxide mask on an amorphous silicon ͑a-Si͒ layer. Results for uncoated fiber probes are compared with those for aluminum-coated probes.…”
Section: Introductionmentioning
confidence: 99%
“…Line scans with an uncoated fiber display a three-peak profile after etching the surface in potassium hydroxide ͑KOH͒. 10 Numerical simulations based on a macroscopic self-consistent model 13,14 have been used to explain the experimental observations. Taking the uncertainty of the precise shape of the probe into account, the model was found to be in good agreement with the observed silicon structures.…”
Optically induced oxidation of hydrogen-passivated silicon surfaces using a scanning near-field optical microscope was achieved with both uncoated and aluminum-coated fiber probes. Line scans on amorphous silicon using uncoated fiber probes display a three-peak profile after etching in potassium hydroxide. Numerical simulations of the electromagnetic field around the probe–sample interaction region are used to explain the experimental observations. With an aluminum-coated fiber probe, lines of 35 nm in width were transferred into the amorphous silicon layer.
“…Kramer et al [26] used HF-passivated and STM-oxidized a-Si H as a resist layer to etch fine metal wires. In a similar approach, Minne et al [27] were successful in patterning a variety of structures (including a 0.1-m gate MOSFET) by using reactive ion etching to selectively etch an AFM-patterned a-Si H resist layer, and Madsen et al have used both optically induced depassivation and the AFM to oxidize and pattern such layers [28]. These accomplishments are significant because they demonstrate a general application of the anodic oxidation and selective etching process to a variety of material systems by using easily deposited a-Si H films as a resist layer.…”
We report the successful metal salt complexation of ultrathin terpolymer films spin-coated onto glass and silicon substrates and the subsequent reduction of the salt to metal clusters. The photolabile polymer consists of a diazosulfonate side chain polymer which may be decomposed under UV irradiation. Initial, complexed and reduced stages are characterized using optical transmission spectroscopy and X-ray photoelectron spectroscopy, while the film surface roughness, morphology and thickness are determined from atomic force microscopy and ellipsometry. On the one hand, our experiments show that nonirradiated diazosulfonate side groups complex with silver acetate provided from solution, and that silver ions chemically reduce when exposed to a sodium borohydride solution. On the other hand, the complete destruction of the photolabile diazosulfonate unit with UV irradiation was proven. Our experimental investigations are the first successful effort for selective metallization of deposited ultrathin diazosulfonate polymer films. Furthermore, we were able to show that the films can be optically structured by writing micrometer-sized patterns with a focused UV laser beam.
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